Abbott Diagnostics Scarborough, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Abbott Diagnostics Scarborough, Inc. has 6 FDA 510(k) cleared medical devices. Based in Scarborough, US.
Latest FDA clearance: Jun 2025. Active since 2019. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Abbott Diagnostics Scarborough, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Abbott Diagnostics Scarborough, Inc.
6 devices
Cleared
Jun 13, 2025
BinaxNOW COVID-19 Ag Card
Microbiology
134d
Cleared
Feb 11, 2025
BinaxNOW™ COVID-19 Antigen Self Test
Microbiology
90d
Cleared
Oct 10, 2023
ID NOW Influenza A & B 2
Microbiology
29d
Cleared
Aug 10, 2023
ID NOW COVID-19 2.0
Microbiology
405d
Cleared
Jun 24, 2022
ID Now Instrument, ID Now Influenza A & B 2, ID NOW Strep A 2
Microbiology
98d
Cleared
Jul 11, 2019
ID NOW Influenza A & B 2
Microbiology
31d